Register

Request-Details

Apply now » Request Closed

Looking for US-based regulatory affairs consultant with oncology and biotech background

  • Clinical development and testing, clinical CRO, Regulatory services - CMC writing - medical writing, Consulting - strategy and development
  • Biopharmaceuticals
  • North America
  • 08/23/2013

Description

We are a EU-based biotech company developing mAb and look for a US based RA consultant who could support us with respect to our programme in order to understand and prepare for US-specific interests, questions and enquiries. We want to be prepared specifically to comply with US-specific clinical demands and understand what requirements FDA has in this field of biotech products for oncology in early development and marketing phase.

You might also be interested in

Requests by service category

Requests by regionRequests by specialty

Outsourcing?

Looking for special service?
Don't spend time on search!

Place Request Anonymously »

Get applications from providers For Free